Total Knee Prosthesis and Method for Total Knee Arthroplasty

ABSTRACT

A prosthetic knee implant for implantation into a mammal, which accommodates an anterior cruciate ligament substitute to provide stability to the knee implant. The prosthetic knee implant includes a femoral component having a pair of condylar surfaces and a tibial component having a surface portion adapted to slidably engage the femoral component upon rotation of the same. The femoral component further includes a central femoral recess between the condyles providing access to the femur for drilling a channel through which a cruciate ligament substitute may be integrated into the femur. The tibial component further includes a center portion defining an aperture through which the ligament substitute maybe threaded through the tibia and integrated therein, or anchored upon its surface. Also disclosed is a method used to replace the total knee joint in a mammal with the improved prosthetic knee implant of the present invention.

This application claims the benefit of filing priority under 35 U.S.C. §119 and 37 C.F.R. §1.78 from U.S. Nonprovisional application Ser. No.12/134,713 filed Jun. 6, 2008, for a Total Knee Prosthesis and Methodfor Total Knee Arthroplasty. All information disclosed in the priorapplication is incorporated herein by reference

FIELD OF INVENTION

The present invention relates generally to prosthetic knee implants andcorresponding surgical methods used to replace the total knee joint in amammal. More particularly, the invention relates to a prosthetic kneeimplant having a femoral component and a tibial component, which areadapted to receive an anterior cruciate ligament substitute for biasingthe femur and tibia together.

BACKGROUND OF INVENTION

Mammalian knees wear out for a variety of reasons, includinginflammation from arthritis, injury, or simple wear and tear. Over thepast 40 years, total knee arthroplasties (commonly referred to as totalknee replacements or “TKR”) have become the standard of care forend-stage arthritis. In most TKR procedures, the natural bearingsurfaces of the upper portion of the tibia (tibial plateau) and thelower portion of the femur (femoral condyles) are resected and replacedwith artificial material. Specifically, approximately between 0.5 to 1.5centimeters of the upper portion of the tibia, including both theintercondylar eminence and the medial and lateral tibial plateaus, areresected, leaving a relatively flat surface onto which a rigid supportmember is affixed. Then, a synthetic surface portion is affixed to thesupport member, with the surface portion simulating the intercondylareminence and the tibial plateaus. A lower end portion of the femur isthen resected, and a member having bearing surfaces replicating thefemoral condyles is then affixed to the remaining end of the femur.

The majority of currently available prosthetic knee implants employedfor TKR do not retain the natural anterior cruciate ligament. Rather,during the implant procedure, the anterior cruciate ligament is eitherremoved or, if preservation is attempted, has been found to ruptureshortly after implant of the prosthesis. This is particularly true forTKR candidates, who often have a sacrificed anterior cruciate ligamentgoing into the surgery. As a result, the mechanical interaction betweenthe femoral and tibial components in a TKR is the primary means tostabilize the anterior-posterior motion of the knee.

Although the existing TKR prostheses succeed in increasing patientmobility, and provide the patient with the desired therapeutic result,at least one significant disadvantage remains. Namely, in a TKR whereinthe anterior cruciate ligament is lacking, the femoral condylestranslate in a posterior direction in full extension and translate in ananterior direction in flexion, which is reverse of the motions in anatural knee joint. Such abnormal translation and pivot shift oftenresults in the patient's compromised functional abilities, such asquadriceps avoidance, and changed upper body mechanics during activitiessuch as stair climbing and rising from a chair. Even asymptomaticpatients show gait abnormalities that could lead to reduced functionalability to perform activities of daily living over time.

Further, abnormal anterior translation of the TKR can lead toaccelerated wear of the prosthesis. Indeed, current TKR prostheses havea functional lifespan of approximately 15 years, such that youngerpatients (who are increasingly receiving TKRs) are more likely torequire revision surgery as they age. The amount of bone loss that isinherent in a TKR makes a revision procedure much more difficult in thefuture as even more bone must be removed.

Existing TKR prostheses attempt to compensate for the loss of theanterior cruciate ligament by containing or limiting the amount ofabnormal translation in the nonstabilized knee. For example, U.S. Pat.No. 5,413,604 discloses a TKR prosthesis wherein the anterior cruciateligament must be sacrificed, thereby resulting in a nonstabilized TKRwith abnormal anterior translation. Without an anterior cruciateligament, the prosthesis relies primarily on the mechanical interactionbetween the femoral and tibial components as a means to accommodate theabnormal anterior translation and stabilize the knee. Similarly, U.S.Pat. No. 7,014,660 discloses a TKR prosthesis that incorporates acontrol arm and stop pin assembly to limit the amount of anteriorsliding movement caused by the lack of the anterior cruciate ligament.Unfortunately, neither prosthesis disclosed in the '604 and '660 patentsactually prevents the abnormal anterior translation of the nonstabilizedTKR; or as shown in recent medical research pertaining to medial andlateral translation of ACL deficient knees, rather, they only attempt toaccommodate or limit it. As a result, the patient's functional abilitiesremain limited, and the prosthesis is subject to premature wear andtear. The U.S. Pat. Nos. 5,413,604 and 7,014,660 are hereby incorporatedby reference in their entireties.

Therefore, there exists a constant need in this art for an improved TKRprosthesis that allows for the replacement of an anterior cruciateligament, and approaches the mobility, stability and longevity of anatural, healthy knee joint.

SUMMARY OF THE INVENTION

The present invention is directed to a prosthetic knee implant, and moreparticularly, to a prosthetic knee implant having a femoral componentincluding a medial and lateral condyle, and a tibial component includinga surface portion adapted to slidably engage the femoral component uponrotation of the same. The femoral component includes diverging curvedmembers extending downward and placed on or near the medial and lateralcondyles. These members define a recess in the lower central portion ofthe femoral component. The tibial component includes a center portiondefining an aperture through the tibial component substantially at itscenter. The central femoral recess and the tibial aperture are adaptedto receive an anterior cruciate ligament substitute for biasing thefemur and the tibia together.

In addition, a method of total knee joint replacement in a mammal ispresented consisting of replacing at least a portion of the lower femurwith the improved prosthetic femoral component; replacing at least aportion of the upper tibia with the improved prosthetic tibialcomponent; engaging a drill alignment guide to the femur between thefemoral condyles and drilling a longitudinal channel through the centralfemoral recess and into the femur; engaging a drill alignment guide tothe tibial component and extending the tibial aperture by drilling alongitudinal channel through the tibia aperture and into the tibia. Themethod further includes threading an anterior cruciate ligamentsubstitute into the femoral channel and into the tibial channel andanchoring a first end of the ligament substitute to bone leaving a freeend; applying tension to the free end; and, anchoring the free end tobone under tension such that said femur and the tibia are biasedtogether.

BRIEF DESCRIPTION OF THE DRAWINGS

A total knee prosthesis apparatus and a method for total kneereplacement incorporating the features of the invention are depicted inthe attached drawings which form a portion of the disclosure andwherein:

FIG. 1 is an anatomical view of a human knee joint having an anteriorcruciate ligament and posterior cruciate ligament;

FIG. 2 is a diagram of a prosthetic knee implant in accordance with apreferred embodiment of the present invention, and implanted at thejoint between a human femur and tibia to provide a total kneereplacement;

FIG. 3 is a perspective view of the prosthetic knee implant of FIG. 2;

FIG. 4 is an exploded perspective view of the tibial component;

FIG. 5 is a partial exploded view of the femoral component;

FIG. 6A is an illustration of the femur of FIG. 2 having the femoralchannel drilled longitudinally through the central femoral recess andinto the femur;

FIG. 6B is an illustration of the femur of FIG. 2 with an aligned drillguide for drilling longitudinally through the central femoral recess andinto the femur.

FIG. 7 is an illustration of the tibia of FIG. 2 having the tibialchannel drilled longitudinally through the tibial aperture and into thetibia;

FIG. 8 is a combined illustration of FIG. 6A and FIG. 7, furtherdepicting the femoral channel and tibial channel in substantialalignment in accordance with a preferred embodiment of the presentinvention;

FIG. 9 illustrates the anterior cruciate ligament substitute with aself-anchoring umbrella-type anchor being threaded downward through thefemoral channel and tibial channel; and

FIG. 10 illustrates the anterior cruciate ligament substitute threadedthrough the femoral and tibial channels, under tension, and anchored tothe exterior surfaces of the femur and tibia with umbrella-type anchors.

DESCRIPTION OF THE PREFERRED EMBODIMENTS

Referring to the drawings for a better understanding of the function andstructure of the invention, FIG. 1 shows a typical patient's naturalknee joint 10 prior to the surgical procedure. Illustrated is upperportion 23 of the tibia 20 the upper portion 26 of the fibula 25, thelower portion 18 of the femur 15, the exterior surface 19 of the femur15, as well as the medial condyle 16 and lateral condyle 17. Theanterior cruciate ligament 11 and the posterior cruciate ligament 14 areseen to be present in the knee joint 10. One end 12 of the anteriorcruciate ligament 11 is attached to the anterior portion of theintercondylar eminence 21 of the tibia 20, and the second end 13 of theanterior cruciate ligament 11 is attached to the posterior portion ofthe medial aspect of the lateral femoral condyle 17, thereby defining anaxis 33 of the anterior cruciate ligament 11. The posterior cruciateligament 14 passes upward and forward on the medial side of the anteriorcruciate ligament 11, extending from behind the intercondylar eminence21 to the lateral side of the medial condyle 16 of the femur 15. Alsoseen is the exterior surface 22 of the tibia 20, the tibial plateau 24,the medial meniscal cartilage 27 and lateral meniscal cartilage 28.

The femur 15 and tibia 20 extend along a mechanical axis 32 which isgenerally parallel to the tibia 20 and passes through the head 30 of thenatural hip joint (not shown). The tibia 20 rotates about an axis 31relative to the lower portion 18 of the femur 15 that bisects thecondyles 16 and 17 and is generally perpendicular to the mechanical axis32. During articulation of the knee joint 10 between flexion andextension, the medial condyle 16 engages the tibia 20 along a medialbearing surface bordered by the medial meniscal cartilage 27, while thelateral condyle 17 engages the tibia 20 along a lateral bearing surfacebordered by the lateral meniscal cartilage 28. The anterior crucialligament 11 limits forward movement of the tibia 20 under the femoralcondyles 16 and 17, while the posterior cruciate ligament 14 limitsbackward movement of the tibia 20 under the femoral condyles 16 and 17.

Referring now to FIG. 2, the natural knee joint 10 has been replaced bya prosthetic knee implant 40 constructed in accordance with a preferredembodiment of the present invention. The prosthetic knee implant 40includes a femoral component 41 affixed to the lower portion 18 of thefemur 15 and a tibial component 60 affixed to the upper portion 23 ofthe tibia 20. The femoral component 41 includes a tibial axis ofrotation 49 relative to the lower portion 18 of the femur 15 that isgenerally perpendicular to the mechanical axis 32 and is also orientedin substantial similarity to axis 31 of FIG. 1.

Referring to FIGS. 3 and 4, the femoral component 41 includes areplacement medial condyle 42 and a replacement lateral condyle 43 ofthe femur 15. Normally, the ends of the femoral condyles 16 and 17 areresected and shaped to receive the femoral component 41 and affixed tothe femur 15 as is known in the art, such as adhesion using bone cementand/or pegs extending into the condyles 16 and 17.

The tibial component 60 includes a surface portion 61 adapted toslidably engage the femoral component 41 upon rotation of the tibia 20about tibial axis 49, in such a manner as to enable the prosthetic kneeimplant 40 to serve as a substitute for the natural knee joint 10 forrelative motion of the femur 15 and tibia 20 between flexion andextension. In a preferred embodiment, the tibial component 60 providesreplacement bearing surfaces in the form of lateral bearing surface 69for engagement by the lateral condyle 43 and medial bearing surface 70for engagement by the medial condyle 42 of the prosthetic knee implant40. The tibial component 60 further includes a center portion 62 thatdefines an aperture 63 through the tibial component 60 substantially atits center. Preferably, the tibial aperture 63 is of sufficient size toaccommodate a replacement anterior cruciate ligament.

Typically, the natural anterior cruciate ligament 11 is removed, alongwith approximately between 0.5 to 1.5 centimeters of the upper portion23 of the tibia 20, including the tibial plateau 24, the intercondylareminence 21, the medial meniscal cartilage 27, and the lateral meniscalcartilage 28, thereby leaving a relatively flat surface onto which thetibial component 60 is affixed. In a preferred embodiment, the tibialcomponent 60 includes a support member in the form of a platform 71having a unitary depending stem 72 inserted into the tibia 20 to assistin the accurate location and affixation of the platform 71 on the tibia20. In a preferred embodiment, a surface portion 61 is secured in placeon platform 71 to be interposed between the femoral component 41 andplatform 71 for providing medial and lateral bearing surfaces 70 and 69and for engagement by the medial condyle 42 and the lateral condyle 43,respectively, to enable articulation of the prosthetic knee implant 40.The condyles 42 and 43 preferably are constructed of a biocompatiblehigh-strength alloy, while the preferred material for the surfaceportion 61 is a synthetic polymeric material, such as high-densitypolyethylene. Surface portion 61 may be secured in place on platform 71by means of any of several securing arrangements as described in greaterdetail in U.S. Pat. No. 5,413,604.

In effecting implant of the prosthetic implant 40, the anterior cruciateligament 11 of the natural knee has been sacrificed. Thus, duringarticulation of the prosthetic implant 40 between flexion and extensionthe condyles 42 and 43 translate in a posterior direction in fullextension and translate in an anterior direction in flexion, asdescribed in greater detail in U.S. Pat. No. 5,413,604, col. 4, lines41-67.

Referring to FIG. 5, the femoral component 41 includes the two divergingcurved medial and lateral condyle members 42,43 that extend downward anddefine a recess 45 in the lower central portion of the femoralcomponent. The central femoral recess 45 provides access to the femur 15between the medial and lateral condyles 16 and 17, now resected in favorof implant condyles 42 and 43. Preferably, the central femoral recess 45is of sufficient size to accommodate the integration of an anteriorcruciate ligament substitute through a channel in the femur, as will bedescribed.

Referring to FIG. 6A, a longitudinal channel 46 is drilled in aconventional manner through the central femoral recess 45 and into thefemur 15. In a preferred embodiment, the femoral channel 46 has loweropening 47 and upper opening 48. Alternatively, femoral channel 46 doesnot extend through the exterior surface 19 of the femur 15 butterminates within the femur 15 bone where it is implanted. The femoralchannel 46 is drilled using a conventional two-step process with theengagement of a drill guide (depicted in FIG. 6B) to the femoralcomponent 41 between the femoral condyles 42 and 43 in the centralfemoral recess 45, followed by a drill 50 to create the femoral channel46 of sufficient size to accommodate an anterior cruciate replacement.In a preferred embodiment, the drill guide (depicted in FIG. 6B) isconfigured to align the femoral channel 46 with the tibial aperture 66,as will be discussed. The femoral channel 46 is typically debrided ofall surrounding debris at upper opening 48, and any sharp edges arechamfered using a conventional bone rasp or reamer.

Referring to FIG. 6B, there is shown a drill guide 51 engaged adjacentto the femoral component 41 to provide a temporary guide for the drill50 while drilling the femoral channel 46 through central femoral recess45. In a preferred embodiment, the guide 51 includes a first sleeve 52and a second sleeve 53 aligned longitudinally along a drilling axis 54.The first sleeve 52 and second sleeve 53 each include an aperture 55 and56 disposed longitudinally along the drilling axis 54 suitable forallowing the passage of a drill bit 50.

Referring to FIG. 7, a longitudinal channel 64 is drilled in aconventional manner into the tibia 20 and through the tibial aperture63. In a preferred embodiment, the tibial channel 64 has lower opening65 and upper opening 66. Alternatively, tibial channel 64 does notextend through the exterior surface 22 of the tibia 20 but terminateswithin the tibia 20 bone and to which it is anchored. The tibial channel64 is drilled using a conventional two-step process with the engagementof a drill guide 51 (FIG. 6B) to the tibial component 60, followed by asubsequent drill 50 to create the tibial channel 64 of sufficient sizeto accommodate an anterior cruciate ligament substitute. The tibialchannel 64 is typically debrided of all surrounding debris at loweropening 65, and any sharp edges are chamfered using a conventional bonerasp. In a preferred embodiment, the surface portion 61 is affixed toplatform 71 after the drilling of the tibial channel 64 to preventdamage to the surface portion 61 during drilling. Preferably, the tibialchannel 64 and the femoral channel 46 are in alignment and are orientedalong an axis generally parallel to the axis 33 of an anatomic anteriorcruciate ligament 11.

As mentioned above, the drill guide 51 (FIG. 6B) may also be engagedwith the tibial component 60 to facilitate drilling of the tibialchannel 64. Specifically, the second sleeve 53 may be adapted to nest inand mate with the tibial aperture 63 to define a drilling axis for thedrill 50 while drilling the tibial channel 64. The tibial channel 64 maybe drilled from the lower opening 65 to the upper opening 66, or viceversa.

Referring to FIG. 8, there is shown a prosthetic knee implant 40constructed in accordance with a preferred embodiment. The femoralchannel 46 extends through the exterior surface 19 of the femur 15having lower opening 47 and upper opening 48. The tibial channel 64extends through the exterior surface 22 of the tibia 20 having loweropening 65 and upper opening 66. Femoral channel 46 and tibial channel64 are preferably in alignment and oriented along an axis 67 generallyparallel to the axis 33 of a natural anterior cruciate ligament 11. Theprosthetic implant 40 is now ready to have an anterior cruciate ligamentsubstitute implanted.

The types of anterior cruciate ligament substitutes that can be used inthe present invention include allografts, autografts, xenografts andsynthetic grafts. Allografts include ligamentous tissue harvested fromcadavers and appropriately treated, disinfected, and sterilized.Autografts consist of the patient's own ligamentous tissue harvestedeither from the patellar tendon or from the hamstring, or othersubstitute. Xenografts include ligamentous tissue harvested from onemammalian species and transplanted into or grafted onto another species,genus, or family (such as from porcupine to a human). Synthetic graftsinclude grafts made from synthetic polymers such as polyurethane,polyethylene, polyester and other conventional biocompatible,bioabsorbable or nonabsorbable polymers and composites.

Referring to FIG. 9, an anterior cruciate ligament substitute 80 isthreaded down into the femoral channel 46 and the tibial channel 64.There are numerous methods and instruments known in the art that may beutilized to thread the anterior cruciate ligament substitute 80, whichinclude the use of a suture passer (such as those disclosed in U.S. Pat.Nos. 5,746,754; 5,439,467; and 5,462,562), a graft-passing wire (such asthat disclosed in U.S. Pat. No. 6,623,524), or a ligature carrier (suchas that disclosed in U.S. Pat. No. 6,245,073 col. 2 lines 23-25) U.S.Pat. Nos. 5,746,754; 5,439,467; 5,462,562; 6,623,524; and 6,245,073 arehereby incorporated by reference in their entirety. Alternatively, thesecond end 82 of the ligament substitute 80 is passed down into theupper opening 48 of the femoral channel 46 until it exits the loweropening 47 of the femoral channel 46. A threading instrument 95 having aproximal handle 96 and a distal notched end 97 for engaging the ligamentsubstitute 80 or a leading guide wire 83 attached to the ligamentsubstitute 80 is provided. The distal end 97 of the threading instrument95 is inserted into the lower opening 65 of the tibial channel 64 and ismoved forward and out of the upper opening 66 of the tibial channel 64.Once the ligament substitute 80 is engaged in the distal notched end 97,the threading instrument 95 is withdrawn from the tibial channel 64,thereby pulling the guide wire 83 and passing the second end 82 of theligament substitute 80 down through the upper opening 66 of the tibialchannel 64 and out the lower opening 65 of the tibial channel 64. Atthat time, the guide wire 83 is removed from the threading instrument95. The first end 81 of the ligament substitute 80 is anchored to thefemur 15 using a conventional securing device such as cross-pins,femoral fasteners, endobuttons, screws, or staples. In a preferredembodiment, the first end 81 of the ligament substitute 80 is anchoredto the exterior surface 19 of the femur 15 with a self-anchoringumbrella anchor 90, as shown. Ideally, the ligament substitute 80 iscoated with a substance that facilitates bone ingrowth into the ligamentsubstitute 80, such as a hydroxyaptite (HA) coating. Then, the secondend 82 of the ligament substitute 80 is placed in tension by the surgeonwhile the second end 82 is anchored to the bone of the tibia 20, therebybiasing the tibia 20 and femur 15 together. The second end 82 of theligament substitute 80 may be anchored to the tibia 20 using aconventional securing device such as tibial fasteners, screws andwashers, or staples. Alternatively, the ligament substitute 80 may beanchored from within the femur 15 and/or tibia 20 bone through use of aconventional securing device such as cross pins (such as those describedin U.S. Pat. No. 7,032,599, col. 2, lines 42-62), screws, or anchors.

Referring to FIG. 10, there is shown a prosthetic knee implant 40constructed in accordance with a preferred embodiment. The first end 81of the ligament substitute 80 is disposed longitudinally through thefemoral channel 46 and anchored to the exterior surface 19 of the femur15, and the second end 82 of the ligament substitute 80 is disposedlongitudinally through the tibial channel 64 and anchored to theexterior surface 22 of the tibia 20 with a self-anchoring umbrellaanchor 90. In the preferred embodiment, the ligament substitute 80 isoriented generally parallel to the axis 33 of the natural anteriorcruciate ligament 11.

A surgical kit useful in practicing the method of total kneearthroplasty of the present invention is anticipated by the inventor.Such a kit would include the components previously described above. Morespecifically, the kit is seen to have a femoral component 41 including areplacement medial condyle 42 and a replacement lateral condyle 43, atibial component 60 including a surface portion 61 adapted to slidablyengage the femoral component 41 upon flexion and extension of thefemoral component 41, an anterior cruciate ligament substitute 80, andmeans to anchor the ligament substitute 80 to the femur 15 and tibia 20,such as staples, screws or self-anchoring umbrella anchors 90. Thetibial component 60 further includes a center portion 62 that defines anaperture 63 through the tibial component 60 substantially at its center.The kit would further include at least one drill guide component 51cooperatively shaped to guide a drill bit through the central femoralrecess 45 adjacent to the femur and through the aperture 63 of thetibial components 60.

As will be apparent to one skilled in the art, various modifications canbe made within the scope of the aforesaid description. Suchmodifications being within the ability of one skilled in the art for apart of the present invention and are embraced by the claims below. Forexample, the inventor anticipates variations in the types of anchorsused, the depth to which any ligament substitute end might be anchoredinside bone, the degree and manner in which tension might be applied toa ligament substitute, and the placement of the apertures in the tibialcomponents 61 and 71 for drilling. The priority in the steps ofanchoring the ligament ends, whether above on the femur or below on thetibia, may be varied in accordance with the surgeon's experience and theparticular operating situation is also anticipated.

1. A prosthetic knee implant, comprising a. a femoral component forfixation to the lower portion of a mammalian femur, said femoralcomponent including a medial and lateral condyle; b. a tibial componentfor fixation to the upper portion of a mammalian tibia, said tibialcomponent including a surface portion adapted to slidably engage saidfemoral component upon rotation of said same; c. wherein said medial andlateral condyles include a bisecting axis around which said tibialcomponent rotates; d. wherein said medial and lateral condyles define afemoral recess disposed substantially within the center of said femoralcomponent; e. wherein said tibial component includes a center portiondefining an aperture through said tibial component substantially at itscenter; and, f. wherein said central femoral recess and said tibialaperture are adapted to receive an anterior cruciate ligament substitutefor biasing said mammalian femur and said mammalian tibia together.
 2. Aprosthetic implant as recited in claim 1, further comprising an anteriorcruciate ligament substitute having one end disposed longitudinallythrough said central femoral recess and anchored to said femur, andhaving its other end disposed longitudinally through said tibialaperture and anchored to said tibia.
 3. A prosthetic implant as recitedin claim 2, wherein each end of said ligament substitute extends througha bone and is anchored onto an exterior surface of said bone.
 4. Aprosthetic implant as recited in claim 3, wherein each end of saidligament substitute includes a self-anchoring umbrella type anchor.
 5. Aprosthetic implant as recited in claim 4, wherein each said aperture isadapted to receive a drill guide.
 6. A prosthetic implant as recited inclaim 5, further comprising a drill guide adapted to cooperativelyengage said central femoral recess for providing a temporary guide fordrilling a channel through said femur, and wherein said drill guide isshaped to have a portion fit between said femoral condyles when engagedwith said central femoral recess.
 7. A prosthetic implant as recited inclaim 1, wherein said medial and lateral condyles axis bisects saidanterior cruciate ligament substitute.
 8. A prosthetic implant asrecited in claim 7, wherein said central femoral recess and said tibialaperture are adapted to receive a drill guide.
 9. A prosthetic implantas recited in claim 8, wherein each said aperture are positionedrelative to one another such that a drilled channel through said tibialaperture and a drilled channel through said femur are in single axisalignment.
 10. The prosthetic implant of claim 1, wherein said femoralchannel and said tibial aperture are oriented along an axis generallyparallel to that of an anatomic anterior cruciate ligament.
 11. Theprosthetic implant of claim 10, further comprising an anterior cruciateligament substitute having one end disposed longitudinally through saidfemoral channel and anchored to said femur, and having its other enddisposed longitudinally through said tibial aperture and anchored tosaid tibia.
 12. The prosthetic implant of claim 11, wherein each end ofsaid ligament substitute extends through a bone and is anchored onto anexterior surface of said bone.
 13. The prosthetic implant of claim 12,wherein each end of said ligament substitute includes a self-anchoringumbrella type anchor.
 14. The invention of claim 1, wherein said centralfemoral recess and said tibial component center portion are orientedalong an axis passing through the anterior part of the intercondylareminence of said tibia and the posterior part of the medial aspect ofsaid lateral femoral condyle.
 15. The prosthetic implant of claim 14,further comprising an anterior cruciate ligament substitute having oneend disposed longitudinally through said central femoral recess andanchored to said femur, and having its other end disposed longitudinallythrough said tibial aperture and anchored to said tibia.
 16. Theprosthetic implant of claim 15 wherein said central femoral recess andsaid tibial aperture are adapted to receive a drill guide.
 17. Aprosthetic knee implant, comprising: a. a femoral component meansaffixed to and replacing a lower portion of a mammalian femur, saidfemoral component means including a medial and lateral condyle; b. atibial component means affixed to and replacing an upper portion of amammalian tibia, said tibial component means including a surface adaptedto slidably engage said femoral component means upon rotation of saidsame; c. wherein said medial and lateral condyles include a bisectingaxis around which said tibial component means rotates; d. wherein saidmedial and lateral condyles define a femoral recess disposedsubstantially within the center of said femoral component means; e.wherein said tibial component means includes a center portion definingan aperture through said tibial component means substantially at itscenter; and, f. wherein said central femoral recess and said aperture insaid tibial component means are adapted to receive an anterior cruciateligament substitute for biasing said mammalian femur and said mammaliantibia together.
 18. A prosthetic implant as recited in claim 17, furthercomprising an anterior cruciate ligament substitute having one enddisposed longitudinally through said central femoral recess and anchoredto said femur, and having its other end disposed longitudinally throughsaid tibial aperture and anchored to said tibia.
 19. A prostheticimplant as recited in claim 18, wherein said central femoral recess andsaid aperture in said tibial component means are adapted to receive adrill guide.
 20. A prosthetic implant as recited in claim 19, whereinsaid femoral component means includes a tibial axis of rotation relativeto the lower end of said femur and bisecting each said condyle of saidfemoral component means, and wherein said central femoral recess ispositioned along said tibial rotation axis.
 21. A method of total kneejoint replacement in a mammal, comprising the steps of: a. replacing atleast a portion of the lower femur with a prosthetic joint component,said femoral component including a medial and lateral condyle andfurther including a recess between said condyles defining a recessextending through the center of said femoral component; b. replacing atleast a portion of the upper tibia with a prosthetic joint component,said tibial component including a surface portion for receiving thesurfaces of said femoral condyles and arranged for slidably supportingsaid same, said tibial component further including an aperturesubstantially at its center; c. engaging a drill alignment guide to saidfemoral component between said femoral condyles and drilling alongitudinal channel through said central femoral recess and into saidfemur; d. engaging a drill alignment guide to said tibial component andextending said tibial aperture by drilling a longitudinal channel intosaid tibia and through said tibial aperture; e. threading an anteriorcruciate ligament substitute into said femoral channel and into saidtibial channel and anchoring a first end of said ligament substitute tobone leaving a free end; f. applying tension to said free end; and, g.anchoring said free end to bone under tension such that said femur andsaid tibia are biased together.
 22. The method as recited in claim 21,further comprising the step of aligning said femoral and tibialchannels.
 23. The method as recited in claim 22, wherein each said stepof drilling a channel further comprises drilling each said channelthrough a bone exterior, and wherein each said step of anchoring saidligament ends further comprises anchoring each end to a bone exterior.24. The method as recited in claim 23, further comprising the step ofattaching one end of said replacement ligament to said bone exterior ofeither said femur or said tibia with a self-anchoring umbrella typeanchor, and attaching said other end of said replacement ligament to abone exterior.
 25. The method as recited in claim 24, wherein said stepof anchoring said first end to bone further comprises anchoring saidfirst end to an exterior of said bone.
 26. A surgical kit for totalreplacement of a knee, comprising: a. a femoral component including amedial and lateral condyle for replacing a lower portion of a mammalianfemur, wherein said medial and lateral condyles define a central femoralrecess disposed vertically through said femoral component; b. a tibialcomponent including a surface portion adapted to slidably engage saidfemoral component upon rotation of said same around said femoralcomponent for replacing an upper portion of a mammalian tibia, saidtibial component including a center portion defining an aperture throughsaid tibial component substantially at its center; c. at least one drillguide component cooperatively shaped to engage said central femoralrecess and said tibial aperture; d. wherein said central femoral recessand said tibial aperture are adapted to receive said drill guidecomponent for stabilizing said same; e. an anterior cruciate ligamentsubstitute component for tensioning a femur against a tibia; and, f.anchoring means for anchoring said ligament substitute to said femur andsaid tibia.
 27. A method of consuming the components of a surgical kitduring total knee replacement surgery, comprising the steps of: a.utilizing the components in a surgical kit, said kit comprising: i. afemoral component including a medial and lateral condyle for replacing alower portion of a mammalian femur, said femoral component including acentral recess located between said medial and lateral condyles anddefining a slot vertically oriented through said femoral component; ii.a tibial component including a surface portion adapted to slidablyengage said femoral component upon rotation of said same around saidfemoral component for replacing an upper portion of a mammalian tibia,said tibial component including a center portion defining an aperturethrough said tibial component substantially at its center; iii. at leastone drill guide component cooperatively shaped to engage said femoralslot and said tibial aperture; iv. wherein said femoral slot and saidtibial aperture are adapted to receive said drill guide component forstabilizing said same; v. an anterior cruciate ligament substitutecomponent for biasing said femur against said tibia; and, vi. anchoringmeans for anchoring said ligament substitute to said femur and saidtibia.